posted on 2019-10-29, 19:03authored byNarmina O. Balayeva, Nan Zheng, Ralf Dillert, Detlef W. Bahnemann
Herein, the visible-light-induced
dehydrogenation of N-heterocycles
such as tetrahydroquinolines, tetrahydroisoquinolines, and indolines
in O2-containing suspensions of a commercially available
titanium dioxide photocatalyst yielding the corresponding heteroarenes
is presented. 4-Amino-2,2,6,6-tetramethylpipiridinyloxyl (4-amino-TEMPO)
was found to exhibit a beneficial role, as it increased the yield
and improved the selectivity of the dehydrogenation reaction. Both
the selectivity and the yield are further enhanced by grafting 0.1
wt % of Ni(II) ions onto the TiO2 surface. It is proposed
that the basic reactant adsorbs at Lewis acid sites present at the
TiO2 surface. The dehydrogenation reaction is initiated
by visible-light excitation of the resulting surface complex and a
subsequent single-electron transfer from the excited N-heterocycle
via the conduction band of TiO2 to O2. Ni(II)
ions possibly serve as an electron transfer bridge between the conduction
band of TiO2 and O2, while the TEMPO derivative
is assumed to act as a selective redox mediator involved in reactions
of the generated reactive oxygen species.